Does MICONAZOLE Cause Product use in unapproved indication? 100 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 100 reports of Product use in unapproved indication have been filed in association with MICONAZOLE (Zeasorb Athletes Foot). This represents 1.7% of all adverse event reports for MICONAZOLE.
100
Reports of Product use in unapproved indication with MICONAZOLE
1.7%
of all MICONAZOLE reports
2
Deaths
2
Hospitalizations
How Dangerous Is Product use in unapproved indication From MICONAZOLE?
Of the 100 reports, 2 (2.0%) resulted in death, 2 (2.0%) required hospitalization, and 1 (1.0%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MICONAZOLE. However, 100 reports have been filed with the FAERS database.
What Other Side Effects Does MICONAZOLE Cause?
Vulvovaginal burning sensation (1,870)
Drug ineffective (1,170)
Vulvovaginal pain (1,036)
Vulvovaginal pruritus (651)
Vaginal haemorrhage (543)
Condition aggravated (524)
Vulvovaginal discomfort (487)
Vulvovaginal swelling (419)
Burning sensation (177)
Vaginal discharge (172)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which MICONAZOLE Alternatives Have Lower Product use in unapproved indication Risk?
MICONAZOLE vs MIDAZOLAM
MICONAZOLE vs MIDAZOLAM\MIDAZOLAM
MICONAZOLE vs MIDODRINE
MICONAZOLE vs MIDOMAFETAMINE
MICONAZOLE vs MIDOSTAURIN